Impaired Muscular Fat Metabolism in Juvenile Idiopathic Arthritis in Inactive Disease
Objectives: The objective of this study was to evaluate muscular metabolic function in children with inactive juvenile idiopathic arthritis (JIA).Methods: Fifteen children with inactive JIA and fifteen healthy controls were matched by sex, biological age, and Tanner stage. Participants completed a s...
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Frontiers Media S.A.
2019-05-01
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Series: | Frontiers in Physiology |
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Online Access: | https://www.frontiersin.org/article/10.3389/fphys.2019.00528/full |
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DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Emmanuelle Rochette Emmanuelle Rochette Emmanuelle Rochette Emmanuelle Rochette Pierre Bourdier Bruno Pereira Stéphane Echaubard Stéphane Echaubard Corinne Borderon Nicolas Caron Aurélie Chausset Aurélie Chausset Daniel Courteix Solenne Fel Justyna Kanold Justyna Kanold Justine Paysal Sébastien Ratel Nadège Rouel Nadège Rouel Catherine Sarret Catherine Sarret Daniel Terral Alexandra Usclade Alexandra Usclade Etienne Merlin Etienne Merlin Etienne Merlin Pascale Duché Pascale Duché Pascale Duché |
spellingShingle |
Emmanuelle Rochette Emmanuelle Rochette Emmanuelle Rochette Emmanuelle Rochette Pierre Bourdier Bruno Pereira Stéphane Echaubard Stéphane Echaubard Corinne Borderon Nicolas Caron Aurélie Chausset Aurélie Chausset Daniel Courteix Solenne Fel Justyna Kanold Justyna Kanold Justine Paysal Sébastien Ratel Nadège Rouel Nadège Rouel Catherine Sarret Catherine Sarret Daniel Terral Alexandra Usclade Alexandra Usclade Etienne Merlin Etienne Merlin Etienne Merlin Pascale Duché Pascale Duché Pascale Duché Impaired Muscular Fat Metabolism in Juvenile Idiopathic Arthritis in Inactive Disease Frontiers in Physiology pediatric physical activity inflammation fat oxidation metabolism |
author_facet |
Emmanuelle Rochette Emmanuelle Rochette Emmanuelle Rochette Emmanuelle Rochette Pierre Bourdier Bruno Pereira Stéphane Echaubard Stéphane Echaubard Corinne Borderon Nicolas Caron Aurélie Chausset Aurélie Chausset Daniel Courteix Solenne Fel Justyna Kanold Justyna Kanold Justine Paysal Sébastien Ratel Nadège Rouel Nadège Rouel Catherine Sarret Catherine Sarret Daniel Terral Alexandra Usclade Alexandra Usclade Etienne Merlin Etienne Merlin Etienne Merlin Pascale Duché Pascale Duché Pascale Duché |
author_sort |
Emmanuelle Rochette |
title |
Impaired Muscular Fat Metabolism in Juvenile Idiopathic Arthritis in Inactive Disease |
title_short |
Impaired Muscular Fat Metabolism in Juvenile Idiopathic Arthritis in Inactive Disease |
title_full |
Impaired Muscular Fat Metabolism in Juvenile Idiopathic Arthritis in Inactive Disease |
title_fullStr |
Impaired Muscular Fat Metabolism in Juvenile Idiopathic Arthritis in Inactive Disease |
title_full_unstemmed |
Impaired Muscular Fat Metabolism in Juvenile Idiopathic Arthritis in Inactive Disease |
title_sort |
impaired muscular fat metabolism in juvenile idiopathic arthritis in inactive disease |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Physiology |
issn |
1664-042X |
publishDate |
2019-05-01 |
description |
Objectives: The objective of this study was to evaluate muscular metabolic function in children with inactive juvenile idiopathic arthritis (JIA).Methods: Fifteen children with inactive JIA and fifteen healthy controls were matched by sex, biological age, and Tanner stage. Participants completed a submaximal incremental exercise test to determine their fat and carbohydrate oxidation rates.Results: Between the two groups, heart rate values and carbohydrate oxidation rates were the same, regardless of the relative intensity of exercise. Lipid oxidation rates were lower in JIA patients, regardless of the percentage of VO2 peak (p < 0.05). Respiratory exchange ratios beyond 50% of VO2 peak were higher in patients with JIA (p < 0.05). Respective maximal fat oxidation rates (MFO) for controls and children with JIA were 218.7 ± 92.2 vs. 157.5 ± 65.9 mg ⋅ min-1 (p = 0.03) and 4.9 ± 1.9 vs. 3.4 ± 1.2 mg ⋅ min-1 ⋅ kg-1 (p = 0.04). There was no difference between the two groups in heart rate, percentage of VO2 peak, or power of exercise to achieve MFO. Controls reached their MFO at an exercise power significantly higher than did JIA subjects (42.8 ± 16.8 and 31.9 ± 9.8 W, p = 0.004).Conclusion: Children with JIA show metabolic disturbance during exercise, even when the disease is considered inactive. This disturbance is seen in a lower lipid oxidation rate during submaximal exercise. |
topic |
pediatric physical activity inflammation fat oxidation metabolism |
url |
https://www.frontiersin.org/article/10.3389/fphys.2019.00528/full |
work_keys_str_mv |
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doaj-5a61269328fc4a56914faf8de7e0941a2020-11-25T00:43:27ZengFrontiers Media S.A.Frontiers in Physiology1664-042X2019-05-011010.3389/fphys.2019.00528435098Impaired Muscular Fat Metabolism in Juvenile Idiopathic Arthritis in Inactive DiseaseEmmanuelle Rochette0Emmanuelle Rochette1Emmanuelle Rochette2Emmanuelle Rochette3Pierre Bourdier4Bruno Pereira5Stéphane Echaubard6Stéphane Echaubard7Corinne Borderon8Nicolas Caron9Aurélie Chausset10Aurélie Chausset11Daniel Courteix12Solenne Fel13Justyna Kanold14Justyna Kanold15Justine Paysal16Sébastien Ratel17Nadège Rouel18Nadège Rouel19Catherine Sarret20Catherine Sarret21Daniel Terral22Alexandra Usclade23Alexandra Usclade24Etienne Merlin25Etienne Merlin26Etienne Merlin27Pascale Duché28Pascale Duché29Pascale Duché30Centre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, FranceCIC 1405, Unité CRECHE, INSERM, Université Clermont Auvergne, Clermont-Ferrand, FranceLaboratoire des Adaptations Métaboliques en Conditions Physiologiques et Physiopathologiques, Université Clermont Auvergne, Clermont-Ferrand, FranceCentre de Recherche en Nutrition Humaine d’Auvergne, Clermont-Ferrand, FranceLaboratoire des Adaptations Métaboliques en Conditions Physiologiques et Physiopathologiques, Université Clermont Auvergne, Clermont-Ferrand, FranceDélégation à la Recherche Clinique et à l‘Innovation, Centre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, FranceCentre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, FranceCIC 1405, Unité CRECHE, INSERM, Université Clermont Auvergne, Clermont-Ferrand, FranceCentre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, FranceCentre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, FranceCentre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, FranceCIC 1405, Unité CRECHE, INSERM, Université Clermont Auvergne, Clermont-Ferrand, FranceLaboratoire des Adaptations Métaboliques en Conditions Physiologiques et Physiopathologiques, Université Clermont Auvergne, Clermont-Ferrand, FranceCentre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, FranceCentre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, FranceCIC 1405, Unité CRECHE, INSERM, Université Clermont Auvergne, Clermont-Ferrand, FranceCentre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, FranceLaboratoire des Adaptations Métaboliques en Conditions Physiologiques et Physiopathologiques, Université Clermont Auvergne, Clermont-Ferrand, FranceCentre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, FranceCIC 1405, Unité CRECHE, INSERM, Université Clermont Auvergne, Clermont-Ferrand, FranceCentre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, FranceCIC 1405, Unité CRECHE, INSERM, Université Clermont Auvergne, Clermont-Ferrand, FranceCentre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, FranceCentre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, FranceCIC 1405, Unité CRECHE, INSERM, Université Clermont Auvergne, Clermont-Ferrand, FranceCentre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, FranceCIC 1405, Unité CRECHE, INSERM, Université Clermont Auvergne, Clermont-Ferrand, FranceINRA, UMR 1019 UNH, ECREIN, Université Clermont Auvergne, Clermont-Ferrand, FranceLaboratoire des Adaptations Métaboliques en Conditions Physiologiques et Physiopathologiques, Université Clermont Auvergne, Clermont-Ferrand, FranceCentre de Recherche en Nutrition Humaine d’Auvergne, Clermont-Ferrand, FranceLaboratoire Impact de l’Activité Physique sur la Santé, Université de Toulon, Toulon, FranceObjectives: The objective of this study was to evaluate muscular metabolic function in children with inactive juvenile idiopathic arthritis (JIA).Methods: Fifteen children with inactive JIA and fifteen healthy controls were matched by sex, biological age, and Tanner stage. Participants completed a submaximal incremental exercise test to determine their fat and carbohydrate oxidation rates.Results: Between the two groups, heart rate values and carbohydrate oxidation rates were the same, regardless of the relative intensity of exercise. Lipid oxidation rates were lower in JIA patients, regardless of the percentage of VO2 peak (p < 0.05). Respiratory exchange ratios beyond 50% of VO2 peak were higher in patients with JIA (p < 0.05). Respective maximal fat oxidation rates (MFO) for controls and children with JIA were 218.7 ± 92.2 vs. 157.5 ± 65.9 mg ⋅ min-1 (p = 0.03) and 4.9 ± 1.9 vs. 3.4 ± 1.2 mg ⋅ min-1 ⋅ kg-1 (p = 0.04). There was no difference between the two groups in heart rate, percentage of VO2 peak, or power of exercise to achieve MFO. Controls reached their MFO at an exercise power significantly higher than did JIA subjects (42.8 ± 16.8 and 31.9 ± 9.8 W, p = 0.004).Conclusion: Children with JIA show metabolic disturbance during exercise, even when the disease is considered inactive. This disturbance is seen in a lower lipid oxidation rate during submaximal exercise.https://www.frontiersin.org/article/10.3389/fphys.2019.00528/fullpediatricphysical activityinflammationfat oxidationmetabolism |